Flir Systems, Inc. MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared laser for Laser Range Finding (LRF). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared laser for Laser Range Finding (LRF).
Brand
Flir Systems, Inc.
Lot Codes / Batch Numbers
n/a
Products Sold
n/a
Flir Systems, Inc. is recalling MilCAM Recon III Model Family of IR Imagers that incorporate a Class I infared laser for Laser Range due to LRF models were sold to non-DoD customers prior to certification and reporting as required in Title 21 of the Code of Federal Regulations, Subchapter . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
LRF models were sold to non-DoD customers prior to certification and reporting as required in Title 21 of the Code of Federal Regulations, Subchapter J, Parts 1000 - 1050 (21 CFR 1000 - 1050). A filter defect allows transmission of laser energy such that the affected LRF would be Class 3B laser product, however the product is reported to CDRH as a Class I product.
Recommended Action
Per FDA guidance
Customers will be notified by a letter instructing them to stop using the LRF, contact a Customer Service Representative, and to detach and return the Laser Range Finder. For each returned LRF, FLIR will provide a certified Class I LRF.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026